Linked Data
dbSNP Id:
rs2110028011
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.55110703C>A , CM000666.2:g.55110703C>A | GRCh38 |
| NC_000004.11:g.55976870C>A , CM000666.1:g.55976870C>A | GRCh37 |
| NC_000004.10:g.55671627C>A | NCBI36 |
| NG_012004.1:g.19893G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000263923.5:c.1042G>T MANE Select | ENSP00000263923.4:p.Val348Phe | |
| ENST00000647068.1:n.1055G>T | ||
| ENST00000263923.4:c.1042G>T | ENSP00000263923.4:p.Val348Phe | |
| ENST00000512566.1:n.1042G>T | ||
| NM_002253.2:c.1042G>T | NP_002244.1:p.Val348Phe | |
| NM_002253.3:c.1042G>T | NP_002244.1:p.Val348Phe | |
| NM_002253.4:c.1042G>T MANE Select | NP_002244.1:p.Val348Phe |